FDA Investigator: Tara C. Singh

- Tara C. Singh first started conducting FDA inspections in 2009, with the last inspection in 2013. Over that time, Tara C. Singh has conducted 98 inspections at 94 companies across 96 sites.

Get Tara Singh's official FDA inspection documents. Gain valuable insights from their Form 483s and EIRs to ace your next inspection.

Documents

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FDA 483 Avera Institutional Review Board, Sioux Falls | 2013

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Tara C. Singh
Medical Devices & Rad Health Form 483

FDA 483 Zeng, Xiaofeng, MD, Clinical Investigator, Beijingshi | 2013

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Tara C. Singh
Human Drug Form 483

FDA 483 Zeng, Xiaofeng, MD, Clinical Investigator, Beijingshi | 2013

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Tara C. Singh
Human Drug Form 483

FDA 483 HealthEast Institutional Review Board, Saint Paul | 2013

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Tara C. Singh
Medical Devices & Rad Health Form 483

FDA 483 3M Company IRB, St. Paul | 2012

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Tara C. Singh
Human Drug Form 483

FDA 483 Advanced Circulatory Systems, Inc., Roseville | 2012

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Tara C. Singh
Medical Devices & Rad Health Form 483

FDA 483 Medtox Laboratories, Inc., Saint Paul | 2012

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Tara C. Singh
Human Drug Form 483

FDA 483 Bellin Health Corporate IRB, Green Bay | 2012

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Tara C. Singh
Human Drug Form 483

Co-Investigators (43)